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Episodic MemoryNCT07442266

The Dynamics of Representational Change Underlying Recall

A study testing Visual Memory Encoding and Retrieval Task During fMRI in people with Episodic Memory, run by Brown University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this clinical trial is to examine how repeated memory retrieval changes visual representations in the brain in healthy adult participants. Specifically, the study aims to determine whether repeated recall strengthens or transforms neural representations in visual cortex compared to a time-matched control… Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Episodic Memory
What is being tested?
Visual Memory Encoding and Retrieval Task During fMRI
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
3 Feb 2026to 17 Sep 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

None listed.

Who cannot join

  • Under the age of 18 or over the age of 40
  • Does not live in the United States or is not a native speaker of English
  • Diagnosis of a neurological disorders, a history of head trauma, or diagnosis of psychiatric disorder
  • Imperfect and uncorrected visual acuity, color blindness, or imperfect hearing
  • Magnetically or mechanically activated implants or other untested metal implants
  • Claustrophobia

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Brown University Magnetic MRI Research Facility

    Providence, Rhode Island, 02906

Other trials in United States

About this study

The goal of this clinical trial is to examine how repeated memory retrieval changes visual representations in the brain in healthy adult participants. Specifically, the study aims to determine whether repeated recall strengthens or transforms neural representations in visual cortex compared to a time-matched control condition. The main questions it aims to answer are: 1) Does repeated retrieval produce cumulative changes in visual cortical representations compared to a control condition matched for elapsed time? 2) Do these representational changes differ for simple spatial stimuli and complex natural images?

Researchers will compare neural activity patterns during repeated retrieval to those during a control retrieval condition to determine whether repeated recall leads to systematic changes in representational structure beyond those attributable to the passage of time. Participants will: 1) complete two fMRI sessions. 2) Undergo a localizer session including anatomical imaging, population receptive field (pRF) mapping, and a visual category localizer task. 3) Study cue-stimulus pairs consisting of either simple spatial patterns or natural images. 4) Recall previously studied stimuli multiple times during repeated and control retrieval conditions while undergoing fMRI scanning. Brain activity patterns during study and recall will be compared to assess how repeated retrieval influences the structure and tuning of visual representations.

Read the detailed description

Two fMRI sessions will be conducted per subject. In the localizer session, the investigators will collect anatomical images and fMRI data necessary to define visual areas in each individual's native brain space. In addition to two high-resolution anatomical images, two short functional tasks will be acquired from every participant: 1) population receptive field (pRF) mapping; 2) visual category localizer. The pRF mapping task will be several runs of a bar aperture drifting across the central 8 degrees of the visual field. This will allow us to estimate the retinotopic sensitivity of individual voxels in visual cortex and draw boundaries between different retinotopic field maps. The visual category localizer will be a block design with different image categories. This will allow us to define higher-level category-selective brain areas.

In the experimental session, the investigators will collect fMRI data while subjects are undergoing perception and recall of the same stimuli. In order to assess whether our findings generalize across simple and complex visual stimuli, two classes of stimuli will be used: simple patterns in discrete spatial locations, following previous work, and natural images. In study blocks, subjects will study cue-stimulus pairs. Colored fixation dots will be used as cues. Stimuli will be from one of the aforementioned classes. In recall blocks, participants will be asked to recall the stimulus given the cue. Recall will happen under one of two conditions: repeated and control. The repeated condition allows us to examine how memory representations evolve with repeated retrieval, while the control condition will provide a matched baseline to assess changes over the same true time interval. For pairs in the repeated condition, participants will recall each stimulus 5 times, interleaved with recalls from other pairs. For pairs in the control condition, participants will recall each stimulus 2 times. Critically, recalls from this condition will be spaced such that they are matched to recalls 1 and 5 from the repeated condition, providing a control for elapsed time. Study and recall blocks will be performed in interleaved order.

Analyses will compare BOLD activity patterns from repeated retrieval, control retrieval, and study conditions. Data from study trials will be averaged to form a single pattern for each stimulus. Retrieval data will be analyzed separately for each stimulus and retrieval attempt in both conditions. For both spatial stimuli and natural images, the investigators will focus on comparing representational changes between repeated and control conditions. Although the specific models used to characterize brain representations differ by stimulus type, the analyses will otherwise follow parallel procedures. For spatial stimuli, the investigators will use a previously published approach that combines pRF estimates with task-based BOLD data to quantify spatial tuning in visual areas. This method assesses the amplitude of the task-evoked BOLD response in each voxel as a function of the distance between the voxel's pRF and the spatial location of the stimulus. The investigators will compare spatial tuning across repeated and control retrieval conditions, as well as with the study condition, to determine whether changes in spatial tuning accumulate over repeated retrieval. For natural images, the investigators will compare the representational structure of BOLD activity patterns to that of a convolutional neural network (CNN) model. Using representational similarity analysis (RSA), the investigators will assess the similarity between CNN-derived embeddings and BOLD activity patterns during both study and recall. Higher correlations with early CNN layers suggest that low-level visual features are represented, while higher correlations with deeper layers indicate the representation of higher-level visual features. The investigators will use this approach to compare correlations from the repeated and control conditions, testing whether representational changes strengthen with repeated retrieval.

Conditions
Episodic Memory
Being tested
Visual Memory Encoding and Retrieval Task During fMRI

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Visual Memory Encoding and Retrieval Task During fMRIBehavioural

    Participants will study cue-stimulus associations and subsequently retrieve the associated stimuli while undergoing fMRI scanning. Retrieval will occur under two conditions: (1) repeated retrieval, in which stimuli are recalled five times, and (2) control retrieval, in which stimuli are recalled twice with timing matched to the repeated condition. Neural activity patterns during study and recall will be measured using BOLD fMRI.

Study groups in NCT07442266
Study groupRoleWhat they receive
Experimental Memory Retrieval TaskExperimentalAll participants will complete a visual memory encoding and retrieval task during fMRI scanning. The study uses a within-subject design in which each participant completes both a repeated retrieval condition and a time-matched control retrieval condition. This design allows comparison of neural representational changes associated with repeated retrieval while controlling for elapsed time.
Receives: Behavioral: Visual Memory Encoding and Retrieval Task During fMRI

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Representational Change in Visual Cortex

    Difference in multivoxel BOLD activity patterns in visual cortex between repeated and control retrieval conditions during fMRI.

    Measured: 1 hour

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Mar 2026
  2. Study start3 Feb 2026
  3. Primary completion17 Sep 2026
  4. Study completion17 Sep 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Model description
Within-subject experimental design in which all participants complete all conditions during fMRI.
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07442266
Sponsor's protocol ID
STUDY00000849
Other IDs
5P30GM149405
Status last verified
Feb 2026
First submitted
24 Feb 2026
Last updated
16 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Visual Memory Encoding and Retrieval Task During fMRI in people with Episodic Memory, run by Brown University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Representational Change in Visual Cortex (time frame: 1 hour). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Oct 2026.

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